Reviews Nortriptyline Hydrochloride Capsules


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Nortriptyline Hydrochloride Drug Description
Nortriptyline Hydrochloride
(nortriptyline hydrochloride) Capsules

Suicidality and Antidepressant Drugs
Antidepressants increased the risk compared to placebo of suicidal thinking
and behavior (suicidality) in children, adolescents, and young adults in short
term studies of major depressive disorder (MDD) and other psychiatric disorders.
Anyone considering the use of nortriptyline hydrochloride or any other antidepressant
in a child, adolescent or young adult must balance this risk with the clinical
need. Short term studies did not show an increase in the risk of suicidality
with antidepressants compared to placebo in adults aged 65 an older. Depression
and certain other psychiatric disorders are themselves associated with increases
in the risk of suicide. Patients of all ages who are started on therapy should
be monitored appropriately and observed closely for clinical worsening, suicidality,
or unusual changes in behavior. Families and caregivers should be advised
of the need for close observation and communication with the prescriber. Nortriptyline
hydrochloride is not approved for use in pediatric patients. (See WARNINGS:
Clinical Worsening and Suicide Risk, PRECAUTIONS: INFORMATION
FOR PATIENTS, and PRECAUTIONS:
Pediatric Use)

DRUG DESCRIPTION
Nortriptyline hydrochloride is 1-Propanamine, 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-,
hydrochloride. The structural formula is represented below:








Nortriptyline Hydrochloride Capsules USP (equivalent to 10 mg, 25 mg, 50 mg
and 75 mg Nortriptyline), for oral administration, contain the following inactive
ingredients: colloidal silicon dioxide, magnesium stearate, pregelatinized starch
and sodium lauryl sulfate. The 10 mg, 25 mg, 50 mg and 75 mg capsule shells
contain: gelatin, methylparaben, propylparaben, sodium lauryl sulfate and titanium
dioxide. They may also contain: benzyl alcohol, butylparaben, edetate calcium
disodium, silicon dioxide or sodium propionate.
The 10 mg, 25 mg and 75 mg capsule shells also contain D&C Yellow No. 10
and FD&C Blue No. 1.Last reviewed on RxList: 4/17/2008




Nortriptyline Hydrochloride Drug Description
Nortriptyline Hydrochloride
(nortriptyline hydrochloride) Capsules

Suicidality and Antidepressant Drugs
Antidepressants increased the risk compared to placebo of suicidal thinking
and behavior (suicidality) in children, adolescents, and young adults in short
term studies of major depressive disorder (MDD) and other psychiatric disorders.
Anyone considering the use of nortriptyline hydrochloride or any other antidepressant
in a child, adolescent or young adult must balance this risk with the clinical
need. Short term studies did not show an increase in the risk of suicidality
with antidepressants compared to placebo in adults aged 65 an older. Depression
and certain other psychiatric disorders are themselves associated with increases
in the risk of suicide. Patients of all ages who are started on therapy should
be monitored appropriately and observed closely for clinical worsening, suicidality,
or unusual changes in behavior. Families and caregivers should be advised
of the need for close observation and communication with the prescriber. Nortriptyline
hydrochloride is not approved for use in pediatric patients. (See WARNINGS:
Clinical Worsening and Suicide Risk, PRECAUTIONS: INFORMATION
FOR PATIENTS, and PRECAUTIONS:
Pediatric Use)

DRUG DESCRIPTION
Nortriptyline hydrochloride is 1-Propanamine, 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-,
hydrochloride. The structural formula is represented below:








Nortriptyline Hydrochloride Capsules USP (equivalent to 10 mg, 25 mg, 50 mg
and 75 mg Nortriptyline), for oral administration, contain the following inactive
ingredients: colloidal silicon dioxide, magnesium stearate, pregelatinized starch
and sodium lauryl sulfate. The 10 mg, 25 mg, 50 mg and 75 mg capsule shells
contain: gelatin, methylparaben, propylparaben, sodium lauryl sulfate and titanium
dioxide. They may also contain: benzyl alcohol, butylparaben, edetate calcium
disodium, silicon dioxide or sodium propionate.
The 10 mg, 25 mg and 75 mg capsule shells also contain D&C Yellow No. 10
and FD&C Blue No. 1.Last reviewed on RxList: 4/17/2008




Nortriptyline Hydrochloride Drug Description
Nortriptyline Hydrochloride
(nortriptyline hydrochloride) Capsules

Suicidality and Antidepressant Drugs
Antidepressants increased the risk compared to placebo of suicidal thinking
and behavior (suicidality) in children, adolescents, and young adults in short
term studies of major depressive disorder (MDD) and other psychiatric disorders.
Anyone considering the use of nortriptyline hydrochloride or any other antidepressant
in a child, adolescent or young adult must balance this risk with the clinical
need. Short term studies did not show an increase in the risk of suicidality
with antidepressants compared to placebo in adults aged 65 an older. Depression
and certain other psychiatric disorders are themselves associated with increases
in the risk of suicide. Patients of all ages who are started on therapy should
be monitored appropriately and observed closely for clinical worsening, suicidality,
or unusual changes in behavior. Families and caregivers should be advised
of the need for close observation and communication with the prescriber. Nortriptyline
hydrochloride is not approved for use in pediatric patients. (See WARNINGS:
Clinical Worsening and Suicide Risk, PRECAUTIONS: INFORMATION
FOR PATIENTS, and PRECAUTIONS:
Pediatric Use)

DRUG DESCRIPTION
Nortriptyline hydrochloride is 1-Propanamine, 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-,
hydrochloride. The structural formula is represented below:








Nortriptyline Hydrochloride Capsules USP (equivalent to 10 mg, 25 mg, 50 mg
and 75 mg Nortriptyline), for oral administration, contain the following inactive
ingredients: colloidal silicon dioxide, magnesium stearate, pregelatinized starch
and sodium lauryl sulfate. The 10 mg, 25 mg, 50 mg and 75 mg capsule shells
contain: gelatin, methylparaben, propylparaben, sodium lauryl sulfate and titanium
dioxide. They may also contain: benzyl alcohol, butylparaben, edetate calcium
disodium, silicon dioxide or sodium propionate.
The 10 mg, 25 mg and 75 mg capsule shells also contain D&C Yellow No. 10
and FD&C Blue No. 1.Last reviewed on RxList: 4/17/2008




Nortriptyline Hydrochloride Drug Description
Nortriptyline Hydrochloride
(nortriptyline hydrochloride) Capsules

Suicidality and Antidepressant Drugs
Antidepressants increased the risk compared to placebo of suicidal thinking
and behavior (suicidality) in children, adolescents, and young adults in short
term studies of major depressive disorder (MDD) and other psychiatric disorders.
Anyone considering the use of nortriptyline hydrochloride or any other antidepressant
in a child, adolescent or young adult must balance this risk with the clinical
need. Short term studies did not show an increase in the risk of suicidality
with antidepressants compared to placebo in adults aged 65 an older. Depression
and certain other psychiatric disorders are themselves associated with increases
in the risk of suicide. Patients of all ages who are started on therapy should
be monitored appropriately and observed closely for clinical worsening, suicidality,
or unusual changes in behavior. Families and caregivers should be advised
of the need for close observation and communication with the prescriber. Nortriptyline
hydrochloride is not approved for use in pediatric patients. (See WARNINGS:
Clinical Worsening and Suicide Risk, PRECAUTIONS: INFORMATION
FOR PATIENTS, and PRECAUTIONS:
Pediatric Use)

DRUG DESCRIPTION
Nortriptyline hydrochloride is 1-Propanamine, 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-,
hydrochloride. The structural formula is represented below:








Nortriptyline Hydrochloride Capsules USP (equivalent to 10 mg, 25 mg, 50 mg
and 75 mg Nortriptyline), for oral administration, contain the following inactive
ingredients: colloidal silicon dioxide, magnesium stearate, pregelatinized starch
and sodium lauryl sulfate. The 10 mg, 25 mg, 50 mg and 75 mg capsule shells
contain: gelatin, methylparaben, propylparaben, sodium lauryl sulfate and titanium
dioxide. They may also contain: benzyl alcohol, butylparaben, edetate calcium
disodium, silicon dioxide or sodium propionate.
The 10 mg, 25 mg and 75 mg capsule shells also contain D&C Yellow No. 10
and FD&C Blue No. 1.Last reviewed on RxList: 4/17/2008




Nortriptyline Hydrochloride Drug Description
Nortriptyline Hydrochloride
(nortriptyline hydrochloride) Capsules

Suicidality and Antidepressant Drugs
Antidepressants increased the risk compared to placebo of suicidal thinking
and behavior (suicidality) in children, adolescents, and young adults in short
term studies of major depressive disorder (MDD) and other psychiatric disorders.
Anyone considering the use of nortriptyline hydrochloride or any other antidepressant
in a child, adolescent or young adult must balance this risk with the clinical
need. Short term studies did not show an increase in the risk of suicidality
with antidepressants compared to placebo in adults aged 65 an older. Depression
and certain other psychiatric disorders are themselves associated with increases
in the risk of suicide. Patients of all ages who are started on therapy should
be monitored appropriately and observed closely for clinical worsening, suicidality,
or unusual changes in behavior. Families and caregivers should be advised
of the need for close observation and communication with the prescriber. Nortriptyline
hydrochloride is not approved for use in pediatric patients. (See WARNINGS:
Clinical Worsening and Suicide Risk, PRECAUTIONS: INFORMATION
FOR PATIENTS, and PRECAUTIONS:
Pediatric Use)

DRUG DESCRIPTION
Nortriptyline hydrochloride is 1-Propanamine, 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-,
hydrochloride. The structural formula is represented below:








Nortriptyline Hydrochloride Capsules USP (equivalent to 10 mg, 25 mg, 50 mg
and 75 mg Nortriptyline), for oral administration, contain the following inactive
ingredients: colloidal silicon dioxide, magnesium stearate, pregelatinized starch
and sodium lauryl sulfate. The 10 mg, 25 mg, 50 mg and 75 mg capsule shells
contain: gelatin, methylparaben, propylparaben, sodium lauryl sulfate and titanium
dioxide. They may also contain: benzyl alcohol, butylparaben, edetate calcium
disodium, silicon dioxide or sodium propionate.
The 10 mg, 25 mg and 75 mg capsule shells also contain D&C Yellow No. 10
and FD&C Blue No. 1.Last reviewed on RxList: 4/17/2008





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Other reviews about Nortriptyline Hydrochloride Capsules on web:

Learn about the prescription medication Nortriptyline Hydrochloride (Nortriptyline Hydrochloride Capsules), drug uses, dosage, side effects, drug interactions, warnings ... Nortriptyline Hydrochloride (Nortriptyline Hydrochloride Capsules ...


Nortriptyline Hydrochloride Pronunciation: (nor-TRIP-tih-leen HIGH-droe-KLOR-ide) Class: Tricyclic compound Trade Names: Aventyl Hydrochloride Pulvules - Capsules 10 mg Complete Nortriptyline Hydrochloride information from Drugs.com


Nortriptyline Hydrochloride Oral capsule To return to the main entry click here . What is this medicine? NORTRIPTYLINE (nor TRIP ti leen) is used to Nortriptyline Hydrochloride Oral capsule: Information from Answers.com


Users share their experience with Nortriptyline Hydrochloride Capsules and comment on drug side effects, effectiveness, and treatment knowledge Nortriptyline Hydrochloride Capsules Drug and Medication User ...


Nortriptyline Hydrochloride Capsules USP (equivalent to 10 mg Nortriptyline) are #3, opaque deep green and opaque white capsules imprinted Nortriptyline and DAN 10 mg supplied in ... Nortriptyline FDA


Nortriptyline Hydrochloride Capsules USP (equivalent to 25 mg Nortriptyline) are #1, opaque deep green and opaque white capsules imprinted Nortriptyline and DAN 25 mg supplied in ... Nortriptyline Official FDA information, side effects and uses.


Common Name: Nortriptyline Hydrochloride Capsules and Tablets Chemical Name: 1-Propanamine, 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-, hydrochloride ... Section 1 - Chemical Product and Company


PAMELOR™ (nortriptyline hydrochloride capsules, USP) 10 mg Covidien Pharmaceuticals - PAMELOR™ 10 mg


30 capsules: $12.99: 60 capsules: $15.98: 90 capsules: $19.97: 100 capsules: $22.19: 120 capsules ... Nortriptyline Hcl 25mg will add to the effects of alcohol and other depressants. Nortriptyline Hcl - drugstore.com. Low prices, side effects ...


Find out all about nortriptyline hydrochloride capsule side effects, including the most common uses, side effects, interactions and risk factors from leading medical experts. Nortriptyline Hydrochloride Capsule Side Effects - a comprehensive ...





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